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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   cutaneous t cell lymphoma
  

Disease ID 846
Disease cutaneous t cell lymphoma
Definition
A group of lymphomas exhibiting clonal expansion of malignant T-lymphocytes arrested at varying stages of differentiation as well as malignant infiltration of the skin. MYCOSIS FUNGOIDES; SEZARY SYNDROME; LYMPHOMATOID PAPULOSIS; and PRIMARY CUTANEOUS ANAPLASTIC LARGE CELL LYMPHOMA are the best characterized of these disorders.
Synonym
cells cutaneous lymphomas t
ctcl
ctcl - cutaneous t-cell lymphoma
cutaneous t-cell lymphoma
cutaneous t-cell lymphoma (morphologic abnormality)
cutaneous t-cell lymphoma, no icd-o subtype
cutaneous t-cell lymphoma, no icd-o subtype (morphologic abnormality)
cutaneous t-cell lymphoma, no international classification of diseases for oncology subtype
cutaneous t-cell lymphoma, no international classification of diseases for oncology subtype (morphologic abnormality)
cutaneous t-cell lymphomas
cutaneous t-cell non-hodgkin lymphoma
cutaneous t-cell non-hodgkin's lymphoma
lymphoma, cutaneous t-cell
lymphoma, t cell, cutaneous
lymphoma, t-cell, cutaneous
lymphoma, t-cell, cutaneous [disease/finding]
lymphomas, cutaneous t-cell
primary cutaneous t-cell lymphoma
primary cutaneous t-cell lymphoma (disorder)
primary cutaneous t-cell non-hodgkin's lymphoma
skin t-cell non-hodgkin's lymphoma
t cell cutaneous lymphoma
t cell lymphoma, cutaneous
t-cell cutaneous lymphoma
t-cell lymphoma, cutaneous
t-cell lymphomas, cutaneous
t-cell non-hodgkin's lymphoma of skin
t-cell non-hodgkin's lymphoma of the skin
Orphanet
DOID
UMLS
C0079773
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:25)
C0026948  |  mycosis fungoides  |  9
C0026946  |  mycosis  |  8
C0036920  |  sezary syndrome  |  3
C0024299  |  lymphoma  |  2
C0004623  |  bacterial infections  |  2
C0004623  |  bacterial infection  |  2
C0018801  |  heart failure  |  1
C0019829  |  hodgkin's disease  |  1
C0040053  |  thrombus  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0023434  |  chronic lymphocytic leukemia  |  1
C0085110  |  severe combined immunodefic  |  1
C0263505  |  alopecia universalis  |  1
C0030326  |  panniculitis  |  1
C0015645  |  fasciitis  |  1
C0042900  |  vitiligo  |  1
C0026764  |  myeloma  |  1
C0037274  |  skin disorder  |  1
C0002170  |  alopecia  |  1
C0037274  |  skin disorders  |  1
C0079773  |  cutaneous t-cell lymphoma  |  1
C0023448  |  lymphocytic leukemia  |  1
C0033860  |  psoriasis  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0018802  |  congestive heart failure  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:21)
673  |  BRAF  |  CTD_human
7128  |  TNFAIP3  |  CTD_human
1493  |  CTLA4  |  CTD_human
7157  |  TP53  |  CTD_human
4170  |  MCL1  |  CTD_human
8289  |  ARID1A  |  CTD_human
5335  |  PLCG1  |  CTD_human
6935  |  ZEB1  |  CTD_human
1029  |  CDKN2A  |  CTD_human
6777  |  STAT5B  |  CTD_human
1788  |  DNMT3A  |  CTD_human
472  |  ATM  |  CTD_human
10664  |  CTCF  |  CTD_human
3662  |  IRF4  |  CTD_human
581  |  BAX  |  CTD_human
84433  |  CARD11  |  CTD_human
355  |  FAS  |  CTD_human
387  |  RHOA  |  CTD_human
4791  |  NFKB2  |  CTD_human
940  |  CD28  |  CTD_human
5588  |  PRKCQ  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:23)
1906  |  EDN1  |  CIPHER
3569  |  IL6  |  CIPHER
4170  |  MCL1  |  CTD_human
7157  |  TP53  |  CTD_human
6777  |  STAT5B  |  CTD_human
1788  |  DNMT3A  |  CTD_human
7128  |  TNFAIP3  |  CTD_human
1493  |  CTLA4  |  CTD_human
4791  |  NFKB2  |  CTD_human
5588  |  PRKCQ  |  CTD_human
940  |  CD28  |  CTD_human
355  |  FAS  |  CTD_human
6935  |  ZEB1  |  CTD_human
581  |  BAX  |  CTD_human
1029  |  CDKN2A  |  CTD_human
84433  |  CARD11  |  CTD_human
472  |  ATM  |  CTD_human
387  |  RHOA  |  CTD_human
3662  |  IRF4  |  CTD_human
673  |  BRAF  |  CTD_human
10664  |  CTCF  |  CTD_human
8289  |  ARID1A  |  CTD_human
5335  |  PLCG1  |  CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:167)
100  |  ADA  |  1.715  |  DISEASES
55811  |  ADCY10  |  1.142  |  DISEASES
51390  |  AIG1  |  2.426  |  DISEASES
238  |  ALK  |  3.248  |  DISEASES
51378  |  ANGPT4  |  1.205  |  DISEASES
64225  |  ATL2  |  1.29  |  DISEASES
567  |  B2M  |  2.141  |  DISEASES
64919  |  BCL11B  |  1.483  |  DISEASES
10018  |  BCL2L11  |  1.523  |  DISEASES
605  |  BCL7A  |  3.067  |  DISEASES
65980  |  BRD9  |  1.572  |  DISEASES
79886  |  CAAP1  |  1.472  |  DISEASES
147968  |  CAPN12  |  2.385  |  DISEASES
84433  |  CARD11  |  2.19  |  DISEASES
841  |  CASP8  |  1.096  |  DISEASES
25901  |  CCDC28A  |  2.109  |  DISEASES
80323  |  CCDC68  |  1.846  |  DISEASES
6364  |  CCL20  |  1.585  |  DISEASES
1232  |  CCR3  |  2.435  |  DISEASES
1233  |  CCR4  |  1.896  |  DISEASES
1237  |  CCR8  |  1.345  |  DISEASES
9332  |  CD163  |  2.197  |  DISEASES
930  |  CD19  |  1.632  |  DISEASES
914  |  CD2  |  4.734  |  DISEASES
50489  |  CD207  |  2.291  |  DISEASES
29126  |  CD274  |  1.187  |  DISEASES
958  |  CD40  |  1.059  |  DISEASES
959  |  CD40LG  |  2.647  |  DISEASES
921  |  CD5  |  4.622  |  DISEASES
1043  |  CD52  |  4.1  |  DISEASES
9308  |  CD83  |  2.014  |  DISEASES
942  |  CD86  |  1.681  |  DISEASES
1029  |  CDKN2A  |  2.123  |  DISEASES
1107  |  CHD3  |  1.267  |  DISEASES
170482  |  CLEC4C  |  1.269  |  DISEASES
1452  |  CSNK1A1  |  1.012  |  DISEASES
1485  |  CTAG1B  |  1.055  |  DISEASES
64693  |  CTAGE1  |  2.197  |  DISEASES
6387  |  CXCL12  |  1.311  |  DISEASES
284340  |  CXCL17  |  1.717  |  DISEASES
4283  |  CXCL9  |  1.848  |  DISEASES
2833  |  CXCR3  |  3.194  |  DISEASES
26052  |  DNM3  |  2.229  |  DISEASES
1791  |  DNTT  |  1.463  |  DISEASES
1803  |  DPP4  |  3.569  |  DISEASES
56940  |  DUSP22  |  2.636  |  DISEASES
10938  |  EHD1  |  1.626  |  DISEASES
8667  |  EIF3H  |  1.29  |  DISEASES
30816  |  ERVW-1  |  2.976  |  DISEASES
355  |  FAS  |  2.803  |  DISEASES
100302740  |  FAS-AS1  |  1.679  |  DISEASES
356  |  FASLG  |  2.433  |  DISEASES
2214  |  FCGR3A  |  2.417  |  DISEASES
115352  |  FCRL3  |  2.017  |  DISEASES
344018  |  FIGLA  |  1.824  |  DISEASES
50943  |  FOXP3  |  3.442  |  DISEASES
6624  |  FSCN1  |  1.071  |  DISEASES
2526  |  FUT4  |  2.247  |  DISEASES
2625  |  GATA3  |  2.023  |  DISEASES
115362  |  GBP5  |  1.766  |  DISEASES
7107  |  GPR137B  |  2.2  |  DISEASES
3065  |  HDAC1  |  3.029  |  DISEASES
3066  |  HDAC2  |  2.388  |  DISEASES
10013  |  HDAC6  |  2.571  |  DISEASES
55869  |  HDAC8  |  1.76  |  DISEASES
9734  |  HDAC9  |  1.638  |  DISEASES
51696  |  HECA  |  3.907  |  DISEASES
3320  |  HSP90AA1  |  1.219  |  DISEASES
3384  |  ICAM2  |  1.211  |  DISEASES
3430  |  IFI35  |  1.511  |  DISEASES
3440  |  IFNA2  |  2.3  |  DISEASES
338376  |  IFNE  |  1.164  |  DISEASES
147920  |  IGFL2  |  2.645  |  DISEASES
3550  |  IK  |  1.222  |  DISEASES
3586  |  IL10  |  2.903  |  DISEASES
3605  |  IL17A  |  2.022  |  DISEASES
112744  |  IL17F  |  2.287  |  DISEASES
3559  |  IL2RA  |  2.988  |  DISEASES
3561  |  IL2RG  |  2.757  |  DISEASES
386653  |  IL31  |  3.411  |  DISEASES
133396  |  IL31RA  |  2.178  |  DISEASES
9235  |  IL32  |  2.132  |  DISEASES
3662  |  IRF4  |  2.062  |  DISEASES
3664  |  IRF6  |  1.288  |  DISEASES
3676  |  ITGA4  |  2.155  |  DISEASES
3683  |  ITGAL  |  1.805  |  DISEASES
3684  |  ITGAM  |  1.352  |  DISEASES
3716  |  JAK1  |  1.877  |  DISEASES
3718  |  JAK3  |  3.691  |  DISEASES
3802  |  KIR2DL1  |  2.557  |  DISEASES
3804  |  KIR2DL3  |  2.521  |  DISEASES
3811  |  KIR3DL1  |  4.171  |  DISEASES
3812  |  KIR3DL2  |  5.638  |  DISEASES
3824  |  KLRD1  |  1.449  |  DISEASES
3909  |  LAMA3  |  1.117  |  DISEASES
54900  |  LAX1  |  2.334  |  DISEASES
3932  |  LCK  |  1.734  |  DISEASES
84946  |  LTV1  |  1.781  |  DISEASES
51213  |  LUZP4  |  1.325  |  DISEASES
4111  |  MAGEA12  |  1.063  |  DISEASES
4216  |  MAP3K4  |  1.329  |  DISEASES
4170  |  MCL1  |  1.013  |  DISEASES
4193  |  MDM2  |  1.036  |  DISEASES
2315  |  MLANA  |  1.127  |  DISEASES
4311  |  MME  |  2.467  |  DISEASES
4507  |  MTAP  |  1.858  |  DISEASES
10608  |  MXD4  |  1.327  |  DISEASES
4601  |  MXI1  |  1.691  |  DISEASES
4602  |  MYB  |  1.146  |  DISEASES
4609  |  MYC  |  2.621  |  DISEASES
26292  |  MYCBP  |  1.398  |  DISEASES
89795  |  NAV3  |  3.914  |  DISEASES
9436  |  NCR2  |  1.281  |  DISEASES
259197  |  NCR3  |  1.026  |  DISEASES
4791  |  NFKB2  |  1.056  |  DISEASES
4942  |  OAT  |  3.366  |  DISEASES
56666  |  PANX2  |  1.211  |  DISEASES
142  |  PARP1  |  1.098  |  DISEASES
5079  |  PAX5  |  1.826  |  DISEASES
5358  |  PLS3  |  4.7  |  DISEASES
5406  |  PNLIP  |  1.969  |  DISEASES
10631  |  POSTN  |  1.081  |  DISEASES
5527  |  PPP2R5C  |  1.512  |  DISEASES
5728  |  PTEN  |  1.32  |  DISEASES
5788  |  PTPRC  |  3.339  |  DISEASES
5793  |  PTPRG  |  1.005  |  DISEASES
5887  |  RAD23B  |  2.047  |  DISEASES
63891  |  RNF123  |  1.895  |  DISEASES
9349  |  RPL23  |  1.441  |  DISEASES
6257  |  RXRB  |  1.011  |  DISEASES
6278  |  S100A7  |  1.055  |  DISEASES
6280  |  S100A9  |  1.805  |  DISEASES
6304  |  SATB1  |  2.537  |  DISEASES
6401  |  SELE  |  2.12  |  DISEASES
259230  |  SGMS1  |  1.453  |  DISEASES
140885  |  SIRPA  |  1.063  |  DISEASES
8631  |  SKAP1  |  1.667  |  DISEASES
23583  |  SMUG1  |  1.336  |  DISEASES
100126781  |  SNAR-F  |  1.342  |  DISEASES
26801  |  SNORD48  |  1.139  |  DISEASES
6693  |  SPN  |  3.254  |  DISEASES
23626  |  SPO11  |  1.372  |  DISEASES
6772  |  STAT1  |  1.791  |  DISEASES
6775  |  STAT4  |  2.995  |  DISEASES
6776  |  STAT5A  |  3.514  |  DISEASES
6847  |  SYCP1  |  2.415  |  DISEASES
6863  |  TAC1  |  1.534  |  DISEASES
7062  |  TCHH  |  1.05  |  DISEASES
7037  |  TFRC  |  1.671  |  DISEASES
387357  |  THEMIS  |  2.57  |  DISEASES
7072  |  TIA1  |  4.327  |  DISEASES
201633  |  TIGIT  |  1.017  |  DISEASES
51284  |  TLR7  |  1.463  |  DISEASES
54106  |  TLR9  |  1.445  |  DISEASES
253582  |  TMEM244  |  2.965  |  DISEASES
7110  |  TMF1  |  3.749  |  DISEASES
7124  |  TNF  |  2.304  |  DISEASES
8764  |  TNFRSF14  |  1.203  |  DISEASES
7133  |  TNFRSF1B  |  1.496  |  DISEASES
7293  |  TNFRSF4  |  1.647  |  DISEASES
9760  |  TOX  |  3.983  |  DISEASES
80342  |  TRAF3IP3  |  2.474  |  DISEASES
80705  |  TSGA10  |  1.751  |  DISEASES
10497  |  UNC13B  |  1.108  |  DISEASES
2547  |  XRCC6  |  1.866  |  DISEASES
6935  |  ZEB1  |  1.164  |  DISEASES
7748  |  ZNF195  |  2.228  |  DISEASES
Locus(Waiting for update.)
Disease ID 846
Disease cutaneous t cell lymphoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:21)
HP:0000989  |  pruritis  |  8
HP:0002664  |  Neoplasia  |  4
HP:0012190  |  T cell lymphoma  |  2
HP:0002665  |  Lymphoma  |  2
HP:0100827  |  Lymphocytosis  |  1
HP:0045029  |  Eosinophilic fasciitis  |  1
HP:0012490  |  Inflammation of fat tissue  |  1
HP:0002289  |  Alopecia, complete  |  1
HP:0002861  |  Melanoma  |  1
HP:0005550  |  Chronic lymphatic leukemia  |  1
HP:0003765  |  Psoriasis  |  1
HP:0001019  |  Exfoliative dermititis  |  1
HP:0012192  |  Cutaneous T-cell lymphoma  |  1
HP:0100537  |  Inflammation of the fascia  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0001635  |  Congestive heart failure  |  1
HP:0007431  |  Congenital ichthyosis  |  1
HP:0008064  |  Ichthyosis  |  1
HP:0001596  |  Hair loss  |  1
HP:0001045  |  Blotchy loss of skin color  |  1
HP:0002958  |  Immune dysregulation  |  1
Disease ID 846
Disease cutaneous t cell lymphoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:15)
C2364133  |  infection
C0702102  |  arthritis mutilans
C0343888  |  cutaneous cryptococcosis
C0162323  |  polyarthritis
C0085077  |  sweet's syndrome
C0037284  |  skin lesions
C0032285  |  pneumoniae
C0029166  |  oral manifestations
C0022504  |  kaposi's varicelliform eruption
C0020676  |  hypothyroidism
C0020097  |  htlv-i
C0017661  |  iga nephropathy
C0007682  |  central nervous system disease
C0007137  |  squamous cell carcinoma
C0003864  |  arthritis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:3)
C0033774  |  pruritus  |  6
C0037285  |  skin manifestations  |  1
C0037284  |  skin lesions  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Disease ID 846
Disease cutaneous t cell lymphoma
Case(Waiting for update.)